Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10101385
rs10101385 		8 118911611 regulatory region variant A/G snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1023940
rs1023940
CCDC170 ; LOC107986528
6 151611643 intron variant A/G snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1036066
rs1036066
WLS ; GNG12-AS1
1 68194522 intron variant A/C snv 0.33
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10464592
rs10464592
SEM1
7 96601374 intron variant G/A snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10493013
rs10493013 		1 22376542 regulatory region variant T/C snv 0.20
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2018
dbSNP: rs10505348
rs10505348
COLEC10
8 118960457 intergenic variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10505351
rs10505351
COLEC10
8 119021759 intron variant C/T snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10507508
rs10507508
LINC02341
13 42395646 intron variant A/G snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10507509
rs10507509
LINC02341
13 42398954 intron variant C/T snv 6.2E-02
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10808100
rs10808100
SEM1 ; LOC105375411
7 96501241 intron variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10872676
rs10872676 		6 151622842 downstream gene variant C/A;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10876432
rs10876432
SP7
12 53338107 intron variant G/A snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs10955908
rs10955908
SAMD12-AS1
8 118892318 intron variant C/A snv 0.34
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10955919
rs10955919
COLEC10
8 119008679 intron variant C/G snv 0.62
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs10955924
rs10955924
COLEC10
8 119041104 intron variant C/A snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1107748
rs1107748
LINC02594
1.000 0.080 17 43696446 intron variant T/C snv 0.54
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11155797
rs11155797
CCDC170
6 151580202 intron variant C/T snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11155811
rs11155811
ESR1
6 151756711 intron variant C/T snv 0.44
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs1124674
rs1124674
ESR1
6 151759600 intron variant T/C;G snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11573829
rs11573829
TNFRSF11B
8 118947384 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11573885
rs11573885
TNFRSF11B
8 118936926 intron variant T/C snv 0.45
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11803476
rs11803476 		1 22376832 regulatory region variant C/T snv 0.15
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11810369
rs11810369 		1 22361158 downstream gene variant G/A snv 0.22
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11840862
rs11840862
LINC02341
13 42382327 intron variant A/G snv 0.56
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009
dbSNP: rs11842146
rs11842146
LINC02341
13 42348370 intron variant C/G;T snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2009 2009